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HgiDII 甲基转移酶与 DNA 和 S-腺苷甲硫氨酸复合物的同源建模和分子动力学模拟:催化机制及与 DNA 的相互作用。

Homology modeling and molecular dynamics simulations of HgiDII methyltransferase in complex with DNA and S-adenosyl-methionine: catalytic mechanism and interactions with DNA.

机构信息

Center for Biologics Evaluation and Research, US FDA, CBER/DBPAP [HFM-443], 1401 Rockville Pike, Rockville, MD, 20852, USA.

出版信息

J Mol Model. 2010 Jul;16(7):1213-22. doi: 10.1007/s00894-009-0632-9. Epub 2009 Dec 22.

Abstract

M.HgiDII is a methyltransferase (MTase) from Herpetosiphon giganteus that recognizes the sequence GTCGAC. This enzyme belongs to a group of MTases that share a high degree of amino acid similarity, albeit none of them has been thoroughly characterized. To study the catalytic mechanism of M.HgiDII and its interactions with DNA, we performed molecular dynamics simulations with a homology model of M.HgiDII complexed with DNA and S-adenosyl-methionine. Our results indicate that M.HgiDII may not rely only on Glu119 to activate the cytosine ring, which is an early step in the catalysis of cytosine methylation; apparently, Arg160 and Arg162 may also participate in the activation by interacting with cytosine O2. Another residue from the catalytic site, Val118, also played a relevant role in the catalysis of M.HgiDII. Val118 interacted with the target cytosine and kept water molecules from accessing the region of the catalytic pocket where Cys79 interacts with cytosine, thus preventing water-mediated disruption of interactions in the catalytic site. Specific recognition of DNA was mediated mainly by amino acids of the target recognition domain, although some amino acids (loop 80-88) of the catalytic domain may also contribute to DNA recognition. These interactions involved direct contacts between M.HgiDII and DNA, as well as indirect contacts through water bridges. Additionally, analysis of sequence alignments with closely related MTases helped us to identify a motif in the TRD of M.HgiDII that may be relevant to specific DNA recognition.

摘要

M.HgiDII 是一种来自 Herpetosiphon giganteus 的甲基转移酶(MTase),能够识别 GTCGAC 序列。这种酶属于一组具有高度氨基酸相似性的 MTases,尽管它们中没有一个得到彻底的表征。为了研究 M.HgiDII 的催化机制及其与 DNA 的相互作用,我们使用 M.HgiDII 与 DNA 和 S-腺苷甲硫氨酸复合物的同源模型进行了分子动力学模拟。我们的结果表明,M.HgiDII 可能不仅依赖于 Glu119 来激活胞嘧啶环,这是胞嘧啶甲基化催化的早期步骤;显然,Arg160 和 Arg162 也可能通过与胞嘧啶 O2 相互作用参与激活。催化位点的另一个残基 Val118 也在 M.HgiDII 的催化中发挥了相关作用。Val118 与靶标胞嘧啶相互作用,并阻止水分子进入催化口袋中 Cys79 与胞嘧啶相互作用的区域,从而防止水分子介导的催化位点相互作用的破坏。DNA 的特异性识别主要由靶标识别结构域的氨基酸介导,尽管催化结构域的一些氨基酸(loop 80-88)也可能有助于 DNA 识别。这些相互作用涉及 M.HgiDII 与 DNA 的直接接触,以及通过水桥的间接接触。此外,与密切相关的 MTases 的序列比对分析帮助我们确定了 M.HgiDII 的 TRD 中的一个基序,该基序可能与特定的 DNA 识别有关。

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